Cytolytic activity of membrane attack complex is modulated by ?
Which of the following statements about interleukin-1 is false?
Which of the following is a superantigen ?
What is the primary use of the Hybridoma technique?
An adolescent male developed vomiting and diarrhea 1 hour after having food from a restaurant. The most likely pathogen is?
What is the typical bacterial count in the duodenum?
Which of the following bacteria is known to exhibit antigenic variation?
Most common organism causing ventilator associated pneumonia -
Which fungus is commonly known as golden yellow jelly fungus?
Maximum density of microfilariae in blood is reported to be between -
NEET-PG 2013 - Microbiology NEET-PG Practice Questions and MCQs
Question 71: Cytolytic activity of membrane attack complex is modulated by ?
- A. Factor I
- B. Factor B
- C. Factor S (vitronectin) (Correct Answer)
- D. Factor H
Explanation: ***Correct Option: Factor S (vitronectin)*** - Vitronectin (S-protein) is a **plasma protein** that directly modulates the **cytolytic activity of the membrane attack complex (MAC)**. - It binds to the **C5b-7 complex** in the fluid phase, preventing its insertion into target cell membranes and thereby blocking the formation of the complete, functional MAC. - By inhibiting membrane insertion of C5b-7, vitronectin prevents the subsequent binding of **C8 and C9**, which are essential for the cytolytic pore formation. - This is a **direct modulation** of MAC's cytolytic activity at the MAC assembly stage. *Incorrect Option: Factor H* - Factor H is a regulatory protein that controls the **alternative pathway** of complement activation by promoting degradation of **C3b**. - By degrading C3b, Factor H prevents formation of **C5 convertase**, thereby reducing downstream MAC formation. - However, Factor H acts **early in the complement cascade** and does not directly modulate the cytolytic activity of already-formed MAC components. - Its effect is on **preventing MAC formation**, not on modulating MAC's cytolytic function itself. *Incorrect Option: Factor I* - Factor I is a **serine protease** that cleaves and inactivates C3b and C4b, requiring cofactors like Factor H or C4bp. - Like Factor H, it regulates complement activation **upstream** of MAC formation. - It does not directly interact with or modulate the cytolytic activity of the MAC. *Incorrect Option: Factor B* - Factor B is a component of the **alternative pathway C3 convertase** (C3bBb). - It **promotes complement activation** rather than modulating MAC's cytolytic activity. - Factor B functions early in the cascade and has no direct role in regulating MAC function.
Question 72: Which of the following statements about interleukin-1 is false?
- A. IL-1 is an endogenous pyrogen.
- B. The primary source of IL-1 is the monocyte-macrophage system.
- C. IL-1 inhibits IL-2 production by T-cells. (Correct Answer)
- D. IL-1 promotes acute phase protein synthesis in the liver.
Explanation: ***IL-1 inhibits IL-2 production by T-cells*** - This statement is false because **IL-1** actually **enhances the production of IL-2** by T-cells, which is crucial for T-cell proliferation and immune response. - **IL-1 acts synergistically with IL-6 and TNF-α** to promote inflammation and immune cell activation, where IL-2 plays a key role. *The primary source of IL-1 is the monocyte-macrophage system* - This statement is true; **monocytes and macrophages** are the main producers of **IL-1α and IL-1β** upon activation by various stimuli. - Other cells, such as neutrophils, dendritic cells, and endothelial cells, can also produce IL-1, but monocytes and macrophages are the predominant source. *IL-1 is an endogenous pyrogen* - This statement is true; **IL-1** is a potent **endogenous pyrogen** that acts on the hypothalamus to induce fever, a hallmark of the acute phase response. - It triggers prostaglandin synthesis in the hypothalamus, leading to an elevation in the body's thermoregulatory set point. *IL-1 promotes acute phase protein synthesis in the liver* - This statement is true; **IL-1** is a key mediator that stimulates **hepatocytes** to produce **acute phase proteins**, such as C-reactive protein and serum amyloid A. - This hepatic response is part of the innate immune system's effort to control infection and inflammation.
Question 73: Which of the following is a superantigen ?
- A. Cholera toxin
- B. Diphtheria toxin
- C. TSST (Correct Answer)
- D. Vero-cytoxin
Explanation: ***TSST*** - **Toxic Shock Syndrome Toxin-1 (TSST-1)** is a classic example of a superantigen produced by *Staphylococcus aureus*. - Superantigens **bind directly to MHC class II molecules and T-cell receptors (TCRs)** outside of the antigen-binding groove, leading to non-specific activation of a large percentage of T cells and a massive release of cytokines. *Cholera toxin* - **Cholera toxin** is an exotoxin produced by *Vibrio cholerae* that causes massive fluid secretion in the intestine by **activating adenylate cyclase** in enterocytes. - It functions by **ADP-ribosylating the Gs alpha subunit**, leading to constitutive activation of cyclic AMP production, but it is not a superantigen. *Diphtheria toxin* - **Diphtheria toxin**, produced by *Corynebacterium diphtheriae*, inhibits protein synthesis in eukaryotic cells by **ADP-ribosylating elongation factor-2 (EF-2)**. - This action leads to cell death and the characteristic pseudomembrane formation in diphtheria, but it does not act as a superantigen. *Vero-cytoxin* - **Vero-cytoxin** (also known as Shiga toxin or Shiga-like toxin) is produced by *E. coli* O157:H7 and other Shiga toxin-producing *E. coli* (STEC). - It inhibits protein synthesis by **cleaving ribosomal RNA**, primarily causing damage to intestinal cells and renal endothelial cells, but it is not a superantigen.
Question 74: What is the primary use of the Hybridoma technique?
- A. Monoclonal antibodies (Correct Answer)
- B. Antigen
- C. Specific antibodies
- D. Cytokines
Explanation: ***Monoclonal antibodies*** - The **hybridoma technique** is primarily used to produce **monoclonal antibodies (MAbs)**, which are highly specific antibodies derived from a single B-cell clone. - These antibodies recognize a **single epitope** on an antigen, providing exceptional specificity and uniformity. - The technique involves **fusing a B-lymphocyte** (antibody-producing cell) with a **myeloma cell** (immortal cancer cell) to create a hybridoma that continuously produces identical antibodies. - This is the **gold standard** for producing large quantities of identical, highly specific antibodies for diagnostic and therapeutic use. *Specific antibodies* - While monoclonal antibodies are indeed specific, this term is **too vague** and could refer to any antibody with specificity, including polyclonal antibodies. - **Polyclonal antibodies** are also specific but are produced through conventional immunization, not the hybridoma technique. - The defining characteristic of the hybridoma technique is that it produces **monoclonal** (single clone) antibodies, not just "specific" ones. *Antigen* - An **antigen** is a molecule that elicits an immune response and is used to immunize animals during antibody production. - However, antigens are the **input** for antibody production, not the **product** of the hybridoma technique. *Cytokines* - **Cytokines** are signaling molecules involved in immune cell communication and regulation. - They are not produced by the hybridoma technique, which is specifically designed for **antibody production**.
Question 75: An adolescent male developed vomiting and diarrhea 1 hour after having food from a restaurant. The most likely pathogen is?
- A. Clostridium perfringens
- B. Vibrio parahaemolyticus
- C. Staphylococcus aureus (Correct Answer)
- D. Salmonella
Explanation: ***Staphylococcus aureus*** - The rapid onset of symptoms (within 1 hour) strongly suggests **pre-formed toxin ingestion**, which is characteristic of *Staphylococcus aureus* food poisoning. - While the typical incubation period is **1-6 hours** (average 2-4 hours), onset within 1 hour can occur with **high toxin loads** in contaminated food. - **Vomiting** is often the predominant symptom, occurring shortly after consuming contaminated food, which distinguishes it from other bacterial causes. *Clostridium perfringens* - Onset of symptoms caused by *Clostridium perfringens* is typically **8-16 hours** after ingestion, which is much longer than observed here. - It primarily causes **diarrhea and abdominal cramps** due to toxin production in the intestine, with minimal vomiting. *Vibrio parahaemolyticus* - Symptoms usually appear **4-96 hours** (average 12-24 hours) after consuming contaminated seafood, which is a longer incubation period than described. - It typically causes **watery diarrhea**, abdominal cramps, nausea, and occasional vomiting, but not within 1 hour. *Salmonella* - The incubation period for *Salmonella* infection is typically **6-72 hours** (average 12-36 hours), making it highly unlikely for symptoms to appear within 1 hour. - **Diarrhea, fever, and abdominal cramps** are common with *Salmonella*, but rapid-onset vomiting from pre-formed toxin is not its mechanism.
Question 76: What is the typical bacterial count in the duodenum?
- A. 10^2 per gram (Correct Answer)
- B. 10^1 per gram
- C. 10^10 per gram
- D. 10^5 per gram
Explanation: ***10^2 per gram*** - The duodenum has a **relatively low bacterial count** (typically 10^2-10^4 CFU/gram) due to the **acidic environment** from gastric acid and **rapid transit** of contents. - A count of **10^2 CFU/gram** represents the **lower end of the normal range** for the proximal duodenum, where gastric acid effects are strongest. - This sparse bacterial population contrasts sharply with the dense colonization seen in the distal gut. *10^1 per gram* - This represents an **extremely low count** more characteristic of the **stomach**, not the duodenum. - Such minimal bacterial presence is due to the **hostile acidic environment** (pH 1-3) in the stomach. - The duodenum, while having low counts, consistently has higher bacterial densities than this. *10^5 per gram* - This count is characteristic of the **distal small intestine (ileum)**, where bacterial concentrations progressively increase. - A bacterial count of **10^5 per gram in the duodenum** would be considered **abnormal** and suggest **small intestinal bacterial overgrowth (SIBO)**. - SIBO occurs when colonic-type bacteria colonize the small intestine inappropriately. *10^10 per gram* - This bacterial density is typical of the **colon** (which harbors 10^11-10^12 CFU/gram), the most densely colonized part of the human gut. - Such a high count in the duodenum would indicate **severe bacterial overgrowth** or gross contamination. - The colon's anaerobic environment supports this massive bacterial population.
Question 77: Which of the following bacteria is known to exhibit antigenic variation?
- A. Yersinia
- B. Bordetella
- C. Brucella
- D. Borrelia (Correct Answer)
Explanation: ***Borrelia*** - *Borrelia* species, particularly *Borrelia burgdorferi* (causing **Lyme disease**), are known for extensive **antigenic variation** of their outer surface proteins (Osps), especially OspC. - This variation helps the bacteria evade the host's immune response, contributing to persistent infection. *Yersinia* - While *Yersinia* species produce various virulence factors, including proteins that interfere with immune cell function, they are not primarily known for the type of rapid and extensive **antigenic variation**seen in *Borrelia*. - Their immune evasion strategies often involve modifying host cell signaling pathways and resisting phagocytosis. *Bordetella* - *Bordetella pertussis*, causative agent of **whooping cough**, varies its expression of adhesins and toxins through **phase variation**, which is a form of phenotypic switching. - However, this is distinct from the frequent and sequential changes in surface antigens (antigenic variation) observed in *Borrelia*. *Brucella* - *Brucella* species are **intracellular pathogens** that primarily evade the immune system by surviving and replicating within host cells. - They do not typically engage in significant **antigenic variation** of their surface components as a primary immune evasion mechanism.
Question 78: Most common organism causing ventilator associated pneumonia -
- A. Legionella
- B. Pneumococcus
- C. Pseudomonas (Correct Answer)
- D. Coagulase negative staphylococcus
Explanation: ***Pseudomonas*** - **Pseudomonas aeruginosa** is one of the most common causes of **ventilator-associated pneumonia (VAP)**, particularly in **late-onset VAP** (≥5 days) and in patients with prolonged mechanical ventilation, prior antibiotic exposure, or underlying lung disease. - Its ability to form **biofilms** and its intrinsic antibiotic resistance contribute to its prevalence in hospital-acquired infections. - Along with **Staphylococcus aureus** (especially MRSA), Pseudomonas is consistently among the leading causes of VAP in ICU settings. *Legionella* - **Legionella** is a less common cause of VAP and is typically associated with contaminated water sources, manifesting as **Legionnaires' disease**. - It usually causes severe, rapidly progressive pneumonia and is often harder to culture than other bacteria. *Pneumococcus* - **Streptococcus pneumoniae (Pneumococcus)** is the most common cause of **community-acquired pneumonia (CAP)**, but it is less frequently implicated in VAP. - While it can cause severe pneumonia and may be seen in **early-onset VAP**, its incidence in late-onset VAP is lower compared to Gram-negative rods like Pseudomonas. *Coagulase negative staphylococcus* - **Coagulase-negative Staphylococci** (e.g., *Staphylococcus epidermidis*) are common **contaminants** in cultures and primarily cause device-related infections, such as those associated with central venous catheters. - They are rarely a primary cause of VAP, as they typically have low virulence in the respiratory tract.
Question 79: Which fungus is commonly known as golden yellow jelly fungus?
- A. T. tonsurans
- B. Tremella mesenterica (Correct Answer)
- C. Epidermophyton floccosum
- D. T. mentagrophytes
Explanation: ***Tremella mesenterica*** - This fungus is commonly referred to as **golden yellow jelly fungus** or **witch's butter** due to its distinctive golden-yellow, gelatinous, and brain-like appearance. - It is a **jelly fungus** that typically grows on dead hardwood branches, especially after rain, and is known for its pliable, quivering texture. *T. tonsurans* - This refers to **Trichophyton tonsurans**, a dermatophytic fungus primarily known for causing **tinea capitis** (ringworm of the scalp). - Its common name relates to its effect on hair, causing breakage and a "black dot" appearance, rather than a golden yellow, jelly-like form. *Epidermophyton floccosum* - This is a dermatophytic fungus that specifically causes infections of the **skin and nails**, particularly **tinea pedis** (athlete's foot) and **tinea cruris** (jock itch). - It does not produce a fruiting body and is not described as a jelly-like fungus. *T. mentagrophytes* - This refers to **Trichophyton mentagrophytes**, another common dermatophyte responsible for various superficial fungal infections, including **tinea pedis**, **tinea corporis**, and **tinea unguium**. - Its clinical presentation is not that of a golden yellow jelly fungus.
Question 80: Maximum density of microfilariae in blood is reported to be between -
- A. 9 pm to 11 pm
- B. 11 pm to 2 am (Correct Answer)
- C. 8 pm to 10 pm
- D. 2 am to 5 am
Explanation: ***11 pm to 2 am*** - This period aligns with the **nocturnal periodicity** of *Wuchereria bancrofti* and *Brugia malayi* microfilariae, which are the most common causes of filariasis. - The microfilariae migrate to the **peripheral circulation** during these hours, making it the optimal time for blood smear collection for diagnosis. *9 pm to 11 pm* - While still within the active period for microfilarial migration, the **peak density** is generally observed slightly later. - Blood drawn during this time might show microfilariae, but in lower concentrations compared to the peak. *8 pm to 10 pm* - This timing is generally a little too early to consistently capture the **highest microfilarial load** in nocturnal periodic infections. - The microfilariae are still in the process of migrating from deeper tissues to the peripheral blood. *2 am to 5 am* - By this time, the microfilarial density in the peripheral blood of **nocturnal periodic species** usually starts to decline. - While some microfilariae may still be present, the count would likely be lower than during the earlier peak hours.